Copper transport and its alterations in Menkes and Wilson diseases
- 13 July 2001
- journal article
- review article
- Published by Elsevier
- Vol. 1360 (1) , 3-16
- https://doi.org/10.1016/s0925-4439(96)00064-6
Abstract
No abstract availableThis publication has 88 references indexed in Scilit:
- The Gene Responsible for LEC Hepatitis, Located on Rat Chromosome 16, Is the Homolog to the Human Wilson Disease GeneBiochemical and Biophysical Research Communications, 1994
- Induction of the Putative Copper ATPases, CopA and Copb, of Enterococcus hirae by Ag+ and Cu2+, and Ag+ Extrusion by CopBBiochemical and Biophysical Research Communications, 1994
- Copper-histidine therapy for Menkes diseasePublished by Elsevier ,1993
- Isolation and Characterization of a Human Liver cDNA as a Candidate Gene for Wilson DiseaseBiochemical and Biophysical Research Communications, 1993
- The Use of Trientine in Preventing the Effects of Interrupting Penicillamine Therapy in Wilson's DiseaseNew England Journal of Medicine, 1987
- Binding and uptake of copper from ceruloplasminBiochemical and Biophysical Research Communications, 1986
- Ceruloplasmin receptors of erythrocytesBiochemical and Biophysical Research Communications, 1984
- X-Linked Cutis LaxaNew England Journal of Medicine, 1980
- The effect of cadmium om intestinal copper absorption and binding in the ratLife Sciences, 1977
- Evidence for ceruloplasmin as a copper transport proteinBiochemical and Biophysical Research Communications, 1975